Isolated abnormal FEF75% detects unsuspected bronchiolar obstruction in CF children
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://www.nature.com/articles/s41390-023-02532-2.pdf
Reference35 articles.
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3. Zemanick, E. T. et al. A Phase 3 open-label study of Elexacaftor/Tezacaftor/Ivacaftor in children 6 through 11 years of age with cystic fibrosis and at least one F508 del- CFTR Allele. Am. J. Respir. Crit. Care Med. 203, 1522–1532 (2021).
4. Schluchter, M. D., Konstan, M. W. & Davis, P. B. Jointly modeling the relationship between survival and pulmonary function in cystic fibrosis patients. Stat. Med. 21, 1271–1287 (2002).
5. Tiddens, H. A. W. M., Donaldson, S. H., Rosenfeld, M. & Pare, P. D. Cystic fibrosis lung disease starts in the small airways: can we treat it more effectively? Pediatr. Pulmonol. 45, 107–111 (2010).
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